Reference for FOXF1. Search for FOXF1

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FOXF1

Alveolar capillary dysplasia

Rare lung disease, present at birth and treatable by lung transplants

transplantation. Most cases of ACD are caused by mutations affecting the gene FOXF1 or its nearby enhancer region. Exactly how these mutations lead to abnormal

Alveolar capillary dysplasia

Alveolar_capillary_dysplasia

FOXF1

Protein-coding gene in the species Homo sapiens

Forkhead box protein F1 (FOXF1) is a protein that in humans is encoded by the FOXF1 gene. This gene belongs to the forkhead family of transcription factors

FOXF1

FENDRR

Non-coding RNA in the species Homo sapiens

FOXF1 adjacent non-coding developmental regulatory RNA is a long non-coding RNA that in humans is encoded by the FENDRR gene. This gene produces a spliced

FENDRR

Pitt–Hopkins syndrome

Medical condition

Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure

Pitt–Hopkins syndrome

Pitt–Hopkins_syndrome

List of human transcription factors

motif from similar protein – High-throughput in vitro [256] BVYTAWRYAAACAD FOXF1 ENSG00000103241 Forkhead Known motif – In vivo/Misc source [257] YRHATAAACAHNB

List of human transcription factors

List_of_human_transcription_factors

Interstitial lung disease

Diseases of the space or tissue between the alveoli of the lungs

(mutations in CSFR2A and/or CSFR2B) Alveolar capillary dysplasia (mutations in FoxF1) Mutations in telomerase reverse transcriptase (TERT) Mutations in telomerase

Interstitial lung disease

Interstitial_lung_disease

Tricho-rhino-phalangeal syndrome Type 1

Medical condition

Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure

Tricho-rhino-phalangeal syndrome Type 1

Tricho-rhino-phalangeal_syndrome_Type_1

Campomelic dysplasia

Medical condition

Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure

Campomelic dysplasia

Campomelic_dysplasia

FOX proteins

Family of transcription factors involved in anatomical development

FOXD4L1, FOXD4L3, FOXD4L4, FOXD4L5, FOXD4L6 FOXE1 (thyroid), FOXE3 (lens) FOXF1 (lung), FOXF2 FOXG1 (brain) FOXH1 (widely expressed) FOXI1 (ear), FOXI2

FOX proteins

FOX_proteins

List of OMIM disorder codes

Alveolar capillary dysplasia with misalignment of pulmonary veins; 265380; FOXF1 Alveolar soft part sarcoma; 606243; ASPSCR1 Alzheimer disease 1, familial;

List of OMIM disorder codes

List_of_OMIM_disorder_codes

List of human protein-coding genes 3

HGNC:31986; Q3SYB3 5803 FOXE1 HGNC:3806; O00358 5804 FOXE3 HGNC:3808; Q13461 5805 FOXF1 HGNC:3809; Q12946 5806 FOXF2 HGNC:3810; Q12947 5807 FOXG1 HGNC:3811; P55316

List of human protein-coding genes 3

List_of_human_protein-coding_genes_3

FANCF

Protein-coding gene in the species Homo sapiens

processes including recovering and stabilizing stalled replication forks. FoxF1 protein also interacts with the FA protein core and induces its binding

FANCF